Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Schistosoma mansoni | calcium-activated potassium channel | 0.4207 | 1 | 1 |
Schistosoma mansoni | hypothetical protein | 0.4207 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.1636 | 0.0613 | 0.0613 |
Echinococcus multilocularis | small conductance calcium activated potassium | 0.4207 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.4207 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
K app (binding) | = 0.04 uM | In vitro displacement of [3H]-OXO-M from muscarinic acetylcholine receptor in rat cortical homogenates | ChEMBL. | 2319559 |
K app (binding) | = 0.04 uM | In vitro displacement of [3H]-OXO-M from muscarinic acetylcholine receptor in rat cortical homogenates | ChEMBL. | 2319559 |
K app (binding) | = 0.73 uM | In vitro for its ability to displace [3H]-NMS from muscarinic acetylcholine receptor in rat cortical homogenates | ChEMBL. | 2319559 |
K app (binding) | = 0.73 uM | In vitro for its ability to displace [3H]-NMS from muscarinic acetylcholine receptor in rat cortical homogenates | ChEMBL. | 2319559 |
Ratio (binding) | = 18 | The ratio of Kapp([3H]-NMS) / Kapp([3H]-OXO-M) was determined | ChEMBL. | 2319559 |
Many chemical entities in TDR Targets come from high-throughput screenings with whole cells or tissue samples, and not all assayed compounds have been tested against a single a single target protein, probably because they get ruled out during screening process. Even if these compounds may have not been of interest in the original screening, they may come as interesting leads for other screening assays. Furthermore, we may be able to propose drug-target associations using chemical similarities and network patterns.
1 literature reference was collected for this gene.